International safety notice
Getinge Cardiosave Hybrid, Cardiosave Rescue Intra-Aortic Balloon Pumps - vedeliku sissetungimine ja elektrooniliste komponentide lühis
Estonia / EMDDB · EST · Nov 1, 2021
Key facts
| Title | Getinge Cardiosave Hybrid, Cardiosave Rescue Intra-Aortic Balloon Pumps - vedeliku sissetungimine ja elektrooniliste komponentide lühis |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Getinge Cardiosave Hybrid, Cardiosave Rescue Intra-Aortic Balloon Pumps |
| Manufacturer | GETINGE CARDIOSAVE HYBRID CARDIOSAVE RESCUE INTRAAORTIC BALLOON PUMPS |
| Models | 0998-00-0800-35, 0998-00-0800-33, 0998-00-0800-75, 10607567113432, 0998-00-0800-34, 0998-00-0800-55, 0998-00-0800-31, 10607567109107, 0998-00-0800-52, 10607567113449, 0998-00-0800-32, 10607567108391 and 15 more |
| Date | Nov 1, 2021 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1